From the Department of Physical and Structural Chemistry (S.C., L.P.,
S.K.S.), Laboratory Animal Science (R.W.C.), and Cardiovascular Pharmacology
(L.V.C., E.H.O.), SmithKline Beecham Pharmaceuticals, King of Prussia, Pa.
Correspondence to Sudeep Chandra, PhD, MC: UW 2940, Department of Physical and Structural Chemistry, SmithKline Beecham Pharmaceuticals, 709, Swedeland Road, King of Prussia, PA 19406. E-mail sudeep-chandra-1{at}sbphrd.com
BackgroundAlleviating vascular
restenosis after percutaneous transluminal
angioplasty remains a formidable challenge. Although multiple factors
have been implicated in the pathophysiology of this vascular remodeling
disorder, only limited therapeutic success has been achieved.
Endothelin (ET)-1 has recently been implicated in the pathogenesis of
neointimal growth. We report the in vivo efficacy of SB
217242, a nonpeptide dual ETA/ETB receptor
antagonist with high oral bioavailability, in the rat
carotid artery balloon angioplasty model.
Methods and ResultsThe lumen volumes of carotid arteries were
estimated serially with magnetic resonance imaging (MRI) at baseline
and at day 7 and day 14 after balloon catheterinduced denudation of
the carotid arterial wall in the rat. Histomorphometric
analysis was performed at day 14 after surgery to quantitate
intimal hyperplasia. Statistical analysis was performed with
ANOVA followed by post hoc Newman-Keuls multiple comparison test. In
comparison to vehicle-treated animals, a 20% protection
(P<0.05) from reduction was shown in the estimated
lumen volume with long-term administration of SB 217242 (15 mg/kg BID
PO). Histologic analyses indicated a 42% decrease
(P<0.05) in neointimal growth. The MRI
lumen volumes had a significant correlation with the corresponding
histologic indices.
ConclusionsSerial MRI provides the opportunity to assess the
progression of vascular lumen volume in vivo after balloon angioplasty.
MRI measurements can, in conjunction with in vitro histologic
measurements, contribute to the understanding of the actions of
pharmacologic agents in experimental models of neointima
formation. With the use of serial MRI and histologic measurements, it
is demonstrated that protection from both lumen volume reduction and
neointima formation is obtained in this model by use of a
potent, nonpeptide dual ETA/ETB receptor
antagonist, SB 217242. Furthermore, this study provides
additional support to the implication of ET-1 in the pathophysiology of
neointima formation.
© 1998 American Heart Association, Inc.
Basic Science Reports
Application of Serial In Vivo Magnetic Resonance Imaging to Evaluate the Efficacy of Endothelin Receptor Antagonist SB 217242 in the Rat Carotid Artery Model of Neointima Formation
Key Words: magnetic resonance imaging angioplasty restenosis endothelin
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